Literature DB >> 2367330

Constant-rate intravenous infusion methods for estimating steady-state volumes of distribution and mean residence times in the body for drugs undergoing reversible metabolism.

H Cheng1, W J Jusko.   

Abstract

Equations for the steady-state volumes of distribution (Vss) and the mean residence times in the body (MRT) are derived for a drug and its metabolite subject to reversible metabolism and separately infused intravenously at a constant rate to steady state of both compounds. The Vss and MRT parameters are functions of the integrals of plasma concentrations, plasma concentrations at steady state, and times to reach steady state of both drug and metabolite. In addition, the MRT values are functions of the infusion rates. These equations were validated by computer simulations and comparison with IV bolus dose parameters. These relationships extend the ability to assess the pharmacokinetics of linear reversible metabolic systems.

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Year:  1990        PMID: 2367330     DOI: 10.1023/a:1015874329265

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  11 in total

1.  ANALYSIS OF OPEN SYSTEMS OF MULTIPLE POOLS BY ADMINISTRATION OF TRACERS AT A CONSTANT RATE OR AS A SINGLE DOSE AS ILLUSTRATED BY PROBLEMS INVOLVING STEROID HORMONES.

Authors:  E GURPIDE; J MANN; S LIEBERMAN
Journal:  J Clin Endocrinol Metab       Date:  1963-11       Impact factor: 5.958

2.  Effect of mode of administration on drug distribution in a two-compartment open system.

Authors:  M Gibaldi
Journal:  J Pharm Sci       Date:  1969-03       Impact factor: 3.534

3.  Mean residence time for drugs subject to reversible metabolism.

Authors:  L Aarons
Journal:  J Pharm Pharmacol       Date:  1987-07       Impact factor: 3.765

4.  LAGRAN program for area and moments in pharmacokinetic analysis.

Authors:  M L Rocci; W J Jusko
Journal:  Comput Programs Biomed       Date:  1983-06

5.  The significance of the arterial-venous plasma concentration difference in clearance studies.

Authors:  W L Chiou; G Lam
Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1982-05

6.  Simplified physiologically based method to estimate steady-state volume of distribution.

Authors:  W L Chiou; G Lam
Journal:  J Pharm Sci       Date:  1981-08       Impact factor: 3.534

7.  Residence time and accumulation of drugs in the body.

Authors:  M Weiss
Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1981-02

8.  Reversible metabolism and pharmacokinetics: application to prednisone-prednisolone.

Authors:  J G Wagner; A R DiSanto; W R Gillespie; K S Albert
Journal:  Res Commun Chem Pathol Pharmacol       Date:  1981-06

9.  Simplified method for estimating volume of distribution at steady state.

Authors:  C R Kowarski; A A Kowarski
Journal:  J Pharm Sci       Date:  1980-10       Impact factor: 3.534

Review 10.  Pathophysiological and disease-induced changes in drug distribution volume: pharmacokinetic implications.

Authors:  U Klotz
Journal:  Clin Pharmacokinet       Date:  1976       Impact factor: 6.447

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  2 in total

Review 1.  Transitioning from Basic toward Systems Pharmacodynamic Models: Lessons from Corticosteroids.

Authors:  Vivaswath S Ayyar; William J Jusko
Journal:  Pharmacol Rev       Date:  2020-04       Impact factor: 25.468

Review 2.  Mean residence time of oral drugs undergoing first-pass and linear reversible metabolism.

Authors:  H Cheng; W J Jusko
Journal:  Pharm Res       Date:  1993-01       Impact factor: 4.200

  2 in total

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